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  1. Autophagy Apoptosis
  2. Autophagy Apoptosis
  3. Dioscin

Dioscin  (Synonyms: 薯蕷皂甙; Collettiside III; CCRIS 4123)

目錄號(hào): HY-N0124 純度: 99.95%
COA 產(chǎn)品使用指南

Dioscin (CCRIS 4123; Collettiside III) 是天然的植物來源的甾體皂苷,針對(duì)多種癌細(xì)胞有較好的抗癌活性。Dioscin 可造成 HeLa 和 SiHa 細(xì)胞的 DNA 損傷,并誘導(dǎo)細(xì)胞凋亡 (apoptosis)。Dioscin 調(diào)節(jié) ROS 介導(dǎo)的 DNA 損傷和線粒體信號(hào)通路,發(fā)揮抗癌活性。

MCE 的所有產(chǎn)品僅用作科學(xué)研究或藥證申報(bào),我們不為任何個(gè)人用途提供產(chǎn)品和服務(wù)

Dioscin Chemical Structure

Dioscin Chemical Structure

CAS No. : 19057-60-4

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Customer Review

Other Forms of Dioscin:

    Dioscin purchased from MCE. Usage Cited in: Int Immunopharmacol. 2023 Feb 19;117:109839.  [Abstract]

    Dioscin-Medium group (5 mg/kg; p.o.; every-two days for 12 weeks) profoundly inhibits the phosphorylation of NF-?B in mice (Fig H and I). Dioscin-Low (Dio-L, 2.5 mg/kg), Dioscin-Medium (Dio-M, 5 mg/kg) and Dioscin-High (Dio-H, 10 mg/Kg).

    Dioscin purchased from MCE. Usage Cited in: Mol Med Rep. 2017 Oct;16(4):4922-4926.  [Abstract]

    Dioscin concentrations of 0.5, 1, 5, 10 and 25 μg/mL promotes the expression of ALP and inhibits the expression of LC3B in MC3T3-E1 cells, in a concentration-dependent manner.
    • 生物活性

    • 純度 & 產(chǎn)品資料

    • 參考文獻(xiàn)

    生物活性

    Dioscin (CCRIS 4123; Collettiside III) is a natural plant-derived steroidal saponin that has good anti-cancer activity against a variety of cancer cells. Dioscin causes DNA damage and induces apoptosis in HeLa and SiHa cells. Dioscin regulates ROS-mediated DNA damage and mitochondrial signaling pathways, exerting anticancer activity[1][2][3][4][5][6].

    細(xì)胞效力
    (Cellular Effect)
    Cell Line Type Value Description References
    A2780 IC50
    0.581 μM
    Compound: Dioscin
    Cytotoxicity against human A2780 cells by MTT assay
    Cytotoxicity against human A2780 cells by MTT assay
    [PMID: 21482468]
    A2780 IC50
    0.87 μM
    Compound: Dioscin
    Cytotoxicity against human A2780 cells by MTT assay
    Cytotoxicity against human A2780 cells by MTT assay
    [PMID: 22429911]
    A2780 IC50
    4.46 μM
    Compound: Dioscin
    Cytotoxicity against human A2780 cells after 72 hrs by MTT assay
    Cytotoxicity against human A2780 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    A549 IC50
    0.454 μM
    Compound: Dioscin
    Cytotoxicity against human A549 cells by MTT assay
    Cytotoxicity against human A549 cells by MTT assay
    [PMID: 21482468]
    A549 IC50
    0.7 μM
    Compound: Dioscin
    Cytotoxicity against human A549 cells after 72 hrs by MTT assay
    Cytotoxicity against human A549 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    A549 IC50
    0.81 μM
    Compound: Dioscin
    Cytotoxicity against human A549 cells by MTT assay
    Cytotoxicity against human A549 cells by MTT assay
    [PMID: 22429911]
    A549 IC50
    4.2 μM
    Compound: dioscin
    Cytotoxicity against human A549 cells by MTT assay
    Cytotoxicity against human A549 cells by MTT assay
    [PMID: 16905317]
    BC1 cell line IC50
    3.8 μM
    Compound: 2
    Cytotoxicity against human BC1 cells after 72 hrs by SRB assay
    Cytotoxicity against human BC1 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    Bel-7402 IC50
    0.23 μM
    Compound: Dioscin
    Cytotoxicity against human Bel7402 cells after 72 hrs by MTT assay
    Cytotoxicity against human Bel7402 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    Bel-7402 IC50
    0.81 μM
    Compound: Dioscin
    Cytotoxicity against human Bel7402 cells by MTT assay
    Cytotoxicity against human Bel7402 cells by MTT assay
    [PMID: 22429911]
    Bel-7402 IC50
    0.93 μM
    Compound: Dioscin
    Cytotoxicity against human Bel7402 cells by MTT assay
    Cytotoxicity against human Bel7402 cells by MTT assay
    [PMID: 21482468]
    BGC-823 IC50
    0.268 μM
    Compound: Dioscin
    Cytotoxicity against human BGC823 cells by MTT assay
    Cytotoxicity against human BGC823 cells by MTT assay
    [PMID: 21482468]
    BGC-823 IC50
    1.08 μM
    Compound: Dioscin
    Cytotoxicity against human BGC823 cells by MTT assay
    Cytotoxicity against human BGC823 cells by MTT assay
    [PMID: 22429911]
    BGC-823 IC50
    2 μM
    Compound: dioscin
    Cytotoxicity against human BGC823 cells by MTT assay
    Cytotoxicity against human BGC823 cells by MTT assay
    [PMID: 16905317]
    BXPC-3 IC50
    0.7 μM
    Compound: Dioscin
    Cytotoxicity against human BxPC3 cells after 72 hrs by MTT assay
    Cytotoxicity against human BxPC3 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    BXPC-3 GI50
    1.3 μg/mL
    Compound: 4, dioscin
    Growth inhibition of humanBxPC3 cells after 48 hrs
    Growth inhibition of humanBxPC3 cells after 48 hrs
    [PMID: 15921418]
    Capan-2 IC50
    0.05 μM
    Compound: Dioscin
    Cytotoxicity against human Capan2 cells after 72 hrs by MTT assay
    Cytotoxicity against human Capan2 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    Col2 IC50
    2.8 μM
    Compound: 2
    Cytotoxicity against human Col2 cells after 72 hrs by SRB assay
    Cytotoxicity against human Col2 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    DU-145 GI50
    > 10 μg/mL
    Compound: 4, dioscin
    Growth inhibition of human DU145 cells after 48 hrs
    Growth inhibition of human DU145 cells after 48 hrs
    [PMID: 15921418]
    HCT-8 IC50
    0.34 μM
    Compound: Dioscin
    Cytotoxicity against human HCT8 cells by MTT assay
    Cytotoxicity against human HCT8 cells by MTT assay
    [PMID: 22429911]
    HCT-8 IC50
    0.351 μM
    Compound: Dioscin
    Cytotoxicity against human HCT8 cells by MTT assay
    Cytotoxicity against human HCT8 cells by MTT assay
    [PMID: 21482468]
    HCT-8 IC50
    0.56 μM
    Compound: Dioscin
    Cytotoxicity against human HCT8 cells after 72 hrs by MTT assay
    Cytotoxicity against human HCT8 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    HeLa IC50
    0.5 μM
    Compound: Dioscin
    Cytotoxicity against human HeLa cells by MTT assay
    Cytotoxicity against human HeLa cells by MTT assay
    [PMID: 22429911]
    HGC-27 IC50
    5.9 μM
    Compound: dioscin
    Cytotoxicity against human HGC27 cells by MTT assay
    Cytotoxicity against human HGC27 cells by MTT assay
    [PMID: 16905317]
    HL-60 IC50
    2 μM
    Compound: 6
    Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
    Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
    [PMID: 12828464]
    HL-60 IC50
    3.8 μM
    Compound: 1
    Cytotoxicity against human HL60 cells assessed as cell viability after 72 hrs by MTT assay
    Cytotoxicity against human HL60 cells assessed as cell viability after 72 hrs by MTT assay
    [PMID: 22405922]
    K562 IC50
    4.7 μM
    Compound: 1
    Cytotoxicity against human K562 cells assessed as cell viability after 48 hrs by MTT assay
    Cytotoxicity against human K562 cells assessed as cell viability after 48 hrs by MTT assay
    [PMID: 23621869]
    K562/Adr IC50
    3.3 μM
    Compound: 1
    Cytotoxicity against human K562/ADR cells assessed as cell viability after 48 hrs by MTT assay
    Cytotoxicity against human K562/ADR cells assessed as cell viability after 48 hrs by MTT assay
    [PMID: 23621869]
    KB IC50
    0.53 μM
    Compound: Dioscin
    Cytotoxicity against human KB cells by MTT assay
    Cytotoxicity against human KB cells by MTT assay
    [PMID: 22429911]
    KB IC50
    20.7 μM
    Compound: 2
    Cytotoxicity against human KB cells after 72 hrs by SRB assay
    Cytotoxicity against human KB cells after 72 hrs by SRB assay
    [PMID: 12088425]
    KB ED50
    21 μM
    Compound: 8
    Growth inhibition of human KB cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
    Growth inhibition of human KB cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
    [PMID: 19161316]
    KB-V1 IC50
    > 23 μM
    Compound: 2
    Cytotoxicity against human KBV1 cells after 72 hrs by SRB assay
    Cytotoxicity against human KBV1 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    KETR3 IC50
    0.447 μM
    Compound: Dioscin
    Cytotoxicity against human Ketr3 cells by MTT assay
    Cytotoxicity against human Ketr3 cells by MTT assay
    [PMID: 21482468]
    KM-20L2 GI50
    1.3 μg/mL
    Compound: 4, dioscin
    Growth inhibition of human KM20L2 cells after 48 hrs
    Growth inhibition of human KM20L2 cells after 48 hrs
    [PMID: 15921418]
    LNCaP IC50
    1.7 μM
    Compound: 2
    Cytotoxicity against human LNCAP cells after 72 hrs by SRB assay
    Cytotoxicity against human LNCAP cells after 72 hrs by SRB assay
    [PMID: 12088425]
    LNCaP ED50
    1.7 μM
    Compound: 8
    Growth inhibition of human LNCAP cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
    Growth inhibition of human LNCAP cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
    [PMID: 19161316]
    Lu1 IC50
    1.2 μM
    Compound: 2
    Cytotoxicity against human Lu1 cells after 72 hrs by SRB assay
    Cytotoxicity against human Lu1 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    Lu1 ED50
    1.2 μM
    Compound: 8
    Growth inhibition of human Lu1 cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
    Growth inhibition of human Lu1 cells xenografted in ip dosed NCr nu/nu mouse administered once daily from day 3 to 6 after implantation measured on day 7 by MTT-based hollow-fiber test
    [PMID: 19161316]
    MCF7 GI50
    0.68 μg/mL
    Compound: 4, dioscin
    Growth inhibition of human MCF7 cells after 48 hrs
    Growth inhibition of human MCF7 cells after 48 hrs
    [PMID: 15921418]
    MCF7 IC50
    0.879 μM
    Compound: Dioscin
    Cytotoxicity against human MCF7 cells by MTT assay
    Cytotoxicity against human MCF7 cells by MTT assay
    [PMID: 21482468]
    MCF7 IC50
    1.03 μM
    Compound: Dioscin
    Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
    Cytotoxicity against human MCF7 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    MCF7 IC50
    22.4 μM
    Compound: 2
    Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay
    Cytotoxicity against human MCF7 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    NCI-H460 GI50
    1.8 μg/mL
    Compound: 4, dioscin
    Growth inhibition of human NCI-H460 cells after 48 hrs
    Growth inhibition of human NCI-H460 cells after 48 hrs
    [PMID: 15921418]
    NCI-H460 IC50
    4.56 μM
    Compound: 12
    Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
    Cytotoxicity against human NCI-H460 cells incubated for 24 hrs by MTT assay
    [PMID: 28606759]
    P388 ED50
    > 10 μg/mL
    Compound: 4, dioscin
    Growth inhibition of mouse P388 cells after 48 hrs
    Growth inhibition of mouse P388 cells after 48 hrs
    [PMID: 15921418]
    P388 IC50
    21.9 μM
    Compound: 2
    Cytotoxicity against mouse P388 cells after 72 hrs by SRB assay
    Cytotoxicity against mouse P388 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    PANC-1 IC50
    0.81 μM
    Compound: Dioscin
    Cytotoxicity against human PANC1 cells after 72 hrs by MTT assay
    Cytotoxicity against human PANC1 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    SF-268 GI50
    1.2 μg/mL
    Compound: 4, dioscin
    Growth inhibition of human SF268 cells after 48 hrs
    Growth inhibition of human SF268 cells after 48 hrs
    [PMID: 15921418]
    SK-MEL-2 IC50
    1.8 μM
    Compound: 2
    Cytotoxicity against human SK-MEL-2 cells after 72 hrs by SRB assay
    Cytotoxicity against human SK-MEL-2 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    SW1990 IC50
    0.5 μM
    Compound: Dioscin
    Cytotoxicity against human SW1990 cells after 72 hrs by MTT assay
    Cytotoxicity against human SW1990 cells after 72 hrs by MTT assay
    [PMID: 19362474]
    SW626 IC50
    3.1 μM
    Compound: 2
    Cytotoxicity against human SW626 cells after 72 hrs by SRB assay
    Cytotoxicity against human SW626 cells after 72 hrs by SRB assay
    [PMID: 12088425]
    體外研究
    (In Vitro)

    Dioscin (1.25-5 μg/mL; 6-24 h) 增加 HeLa 和 SiHa 細(xì)胞內(nèi)鈣離子水平,并誘導(dǎo)細(xì)胞凋亡[4]。
    Dioscin (1.25-5 μg/mL; 6-24 h) Dioscin 上調(diào) Bak、Bax、Bid、p53、caspase-3、caspase-9 的蛋白水平,并下調(diào) Bcl-2Bcl-xl 的蛋白水平[4]。

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    體內(nèi)研究
    (In Vivo)

    Dioscin (75-300 mg/kg, 10 mL/kg; oral gavage;90 天) 對(duì)雌性大鼠無亞慢性毒性,對(duì)雄性大鼠有輕微的亞慢性毒性。Dioscin 造成雄性大鼠輕微的胃腸道擴(kuò)張,并且在血液學(xué)評(píng)估中表現(xiàn)出溶血性貧血[5]。
    Dioscin 通過抑制氧化-硝化應(yīng)激、炎癥和細(xì)胞凋亡,可減輕大鼠肝缺血再灌注損傷[6]。

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    分子量

    869.04

    Formula

    C45H72O16

    CAS 號(hào)
    性狀

    固體

    顏色

    White to off-white

    中文名稱

    薯蕷皂甙;薯蕷皂甙; 薯蕷皂苷

    結(jié)構(gòu)分類
    初始來源
    運(yùn)輸條件

    Room temperature in continental US; may vary elsewhere.

    儲(chǔ)存方式
    Powder -20°C 3 years
    4°C 2 years
    In solvent -80°C 2 years
    -20°C 1 year
    溶解性數(shù)據(jù)
    細(xì)胞實(shí)驗(yàn): 

    DMSO 中的溶解度 : ≥ 100 mg/mL (115.07 mM; 吸濕的 DMSO 對(duì)產(chǎn)品的溶解度有顯著影響,請(qǐng)使用新開封的 DMSO)

    * "≥" means soluble, but saturation unknown.

    配制儲(chǔ)備液
    濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg
    1 mM 1.1507 mL 5.7535 mL 11.5070 mL
    5 mM 0.2301 mL 1.1507 mL 2.3014 mL
    查看完整儲(chǔ)備液配制表

    * 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效。
    儲(chǔ)備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲(chǔ)存時(shí),請(qǐng)?jiān)?年內(nèi)使用, -20°C儲(chǔ)存時(shí),請(qǐng)?jiān)?年內(nèi)使用。

    • 摩爾計(jì)算器

    • 稀釋計(jì)算器

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    質(zhì)量
    =
    濃度
    ×
    體積
    ×
    分子量 *

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    濃度 (start)

    C1

    ×
    體積 (start)

    V1

    =
    濃度 (final)

    C2

    ×
    體積 (final)

    V2

    動(dòng)物實(shí)驗(yàn):

    請(qǐng)根據(jù)您的 實(shí)驗(yàn)動(dòng)物和給藥方式 選擇適當(dāng)?shù)娜芙夥桨浮?

    以下溶解方案都請(qǐng)先按照 In Vitro 方式配制澄清的儲(chǔ)備液,再依次添加助溶劑:
    ——為保證實(shí)驗(yàn)結(jié)果的可靠性,澄清的儲(chǔ)備液可以根據(jù)儲(chǔ)存條件,適當(dāng)保存;體內(nèi)實(shí)驗(yàn)的工作液,建議您現(xiàn)用現(xiàn)配,當(dāng)天使用
    以下溶劑前顯示的百分比是指該溶劑在您配制終溶液中的體積占比;如在配制過程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過加熱和/或超聲的方式助溶

    • 方案 一

      請(qǐng)依序添加每種溶劑: 10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: ≥ 2.25 mg/mL (2.59 mM); 澄清溶液

      此方案可獲得 ≥ 2.25 mg/mL(飽和度未知)的澄清溶液。

      1 mL 工作液為例,取 100 μL 22.5 mg/mL 的澄清 DMSO 儲(chǔ)備液加到 400 μL PEG300 中,混合均勻;再向上述體系中加入 50 μL Tween-80,混合均勻;然后再繼續(xù)加入 450 μL 生理鹽水 定容至 1 mL

      生理鹽水的配制:將 0.9 g 氯化鈉,溶解于 ddH?O 并定容至 100 mL,可以得到澄清透明的生理鹽水溶液。
    • 方案 二

      請(qǐng)依序添加每種溶劑: 10% DMSO    90% (20% SBE-β-CD in Saline)

      Solubility: ≥ 2.25 mg/mL (2.59 mM); 澄清溶液

      此方案可獲得 ≥ 2.25 mg/mL(飽和度未知)的澄清溶液。

      1 mL 工作液為例,取 100 μL 22.5 mg/mL 的澄清 DMSO 儲(chǔ)備液加到 900 μL 20% 的 SBE-β-CD 生理鹽水水溶液 中,混合均勻。

      2 g SBE-β-CD(磺丁基醚 β-環(huán)糊精)粉末定容于 10 mL 的生理鹽水中,完全溶解至澄清透明。

    以下溶解方案,請(qǐng)直接配制工作液。建議現(xiàn)用現(xiàn)配,在短期內(nèi)盡快用完。 以下溶劑前顯示的百分比是指該溶劑在您配制終溶液中的體積占比; 如在配制過程中出現(xiàn)沉淀、析出現(xiàn)象,可以通過加熱和/或超聲的方式助溶。

    • 方案 一

      請(qǐng)依序添加每種溶劑: 0.5% CMC-Na/saline water

      Solubility: 5 mg/mL (5.75 mM); 懸濁液; 超聲助溶

    動(dòng)物溶解方案計(jì)算器
    請(qǐng)輸入動(dòng)物實(shí)驗(yàn)的基本信息:

    給藥劑量

    mg/kg

    動(dòng)物的平均體重

    g

    每只動(dòng)物的給藥體積

    μL

    動(dòng)物數(shù)量

    由于實(shí)驗(yàn)過程有損耗,建議您多配一只動(dòng)物的量
    請(qǐng)輸入您的動(dòng)物體內(nèi)配方組成:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    如果您的動(dòng)物是免疫缺陷鼠或者體弱鼠,建議 DMSO 中的在最后工作液體系中的占比盡量不超過 2%。
    方案所需 助溶劑 包括:DMSO ,均可在 MCE 網(wǎng)站選購(gòu)。 Tween 80,均可在 MCE 網(wǎng)站選購(gòu)。
    計(jì)算結(jié)果
    工作液所需濃度 : mg/mL
    儲(chǔ)備液配制方法 : mg 藥物溶于 μL  DMSO(母液濃度為 mg/mL)。
    您所需的儲(chǔ)備液濃度超過該產(chǎn)品的實(shí)測(cè)溶解度,以下方案僅供參考,如有需要,請(qǐng)與 MCE 中國(guó)技術(shù)支持聯(lián)系。
    動(dòng)物實(shí)驗(yàn)體內(nèi)工作液的配制方法 : 取 μL DMSO 儲(chǔ)備液,加入 μL 。 μL ,混合均勻至澄清,再加 μL Tween 80,混合均勻至澄清,再加 μL 生理鹽水。
    連續(xù)給藥周期超過半月以上,請(qǐng)謹(jǐn)慎選擇該方案。
    請(qǐng)確保第一步儲(chǔ)備液溶解至澄清狀態(tài),從左到右依次添加助溶劑。您可采用超聲加熱 (超聲清洗儀,建議頻次 20-40 kHz),渦旋吹打等方式輔助溶解。
    純度 & 產(chǎn)品資料

    純度: 99.95%

    參考文獻(xiàn)

    完整儲(chǔ)備液配制表

    * 請(qǐng)根據(jù)產(chǎn)品在不同溶劑中的溶解度選擇合適的溶劑配制儲(chǔ)備液;一旦配成溶液,請(qǐng)分裝保存,避免反復(fù)凍融造成的產(chǎn)品失效
    儲(chǔ)備液的保存方式和期限:-80°C, 2 years; -20°C, 1 year。-80°C儲(chǔ)存時(shí),請(qǐng)?jiān)?年內(nèi)使用, -20°C儲(chǔ)存時(shí),請(qǐng)?jiān)?年內(nèi)使用。

    可選溶劑 濃度 溶劑體積 質(zhì)量 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 1.1507 mL 5.7535 mL 11.5070 mL 28.7674 mL
    5 mM 0.2301 mL 1.1507 mL 2.3014 mL 5.7535 mL
    10 mM 0.1151 mL 0.5753 mL 1.1507 mL 2.8767 mL
    15 mM 0.0767 mL 0.3836 mL 0.7671 mL 1.9178 mL
    20 mM 0.0575 mL 0.2877 mL 0.5753 mL 1.4384 mL
    25 mM 0.0460 mL 0.2301 mL 0.4603 mL 1.1507 mL
    30 mM 0.0384 mL 0.1918 mL 0.3836 mL 0.9589 mL
    40 mM 0.0288 mL 0.1438 mL 0.2877 mL 0.7192 mL
    50 mM 0.0230 mL 0.1151 mL 0.2301 mL 0.5753 mL
    60 mM 0.0192 mL 0.0959 mL 0.1918 mL 0.4795 mL
    80 mM 0.0144 mL 0.0719 mL 0.1438 mL 0.3596 mL
    100 mM 0.0115 mL 0.0575 mL 0.1151 mL 0.2877 mL
    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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